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Gene: TNS3 |
Gene summary for TNS3 |
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Gene information | Species | Human | Gene symbol | TNS3 | Gene ID | 64759 |
Gene name | tensin 3 | |
Gene Alias | TEM6 | |
Cytomap | 7p12.3 | |
Gene Type | protein-coding | GO ID | GO:0006793 | UniProtAcc | Q68CZ2 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
64759 | TNS3 | HTA11_347_2000001011 | Human | Colorectum | AD | 8.95e-03 | 4.28e-01 | -0.1954 |
64759 | TNS3 | HTA11_696_2000001011 | Human | Colorectum | AD | 3.53e-05 | 4.66e-01 | -0.1464 |
64759 | TNS3 | HTA11_99999970781_79442 | Human | Colorectum | MSS | 3.67e-02 | -2.89e-01 | 0.294 |
64759 | TNS3 | HTA11_99999965062_69753 | Human | Colorectum | MSI-H | 1.81e-07 | 1.11e+00 | 0.3487 |
64759 | TNS3 | HTA11_99999965104_69814 | Human | Colorectum | MSS | 3.89e-14 | 1.02e+00 | 0.281 |
64759 | TNS3 | F007 | Human | Colorectum | FAP | 3.77e-06 | 3.91e-01 | 0.1176 |
64759 | TNS3 | A002-C-010 | Human | Colorectum | FAP | 2.91e-04 | 1.66e-01 | 0.242 |
64759 | TNS3 | A001-C-207 | Human | Colorectum | FAP | 1.01e-03 | -1.05e-01 | 0.1278 |
64759 | TNS3 | A015-C-203 | Human | Colorectum | FAP | 5.74e-29 | -3.06e-02 | -0.1294 |
64759 | TNS3 | A015-C-204 | Human | Colorectum | FAP | 4.48e-05 | -6.53e-02 | -0.0228 |
64759 | TNS3 | A014-C-040 | Human | Colorectum | FAP | 9.01e-03 | 5.14e-03 | -0.1184 |
64759 | TNS3 | A002-C-201 | Human | Colorectum | FAP | 1.03e-11 | -1.94e-01 | 0.0324 |
64759 | TNS3 | A001-C-119 | Human | Colorectum | FAP | 1.83e-06 | -4.31e-02 | -0.1557 |
64759 | TNS3 | A001-C-108 | Human | Colorectum | FAP | 2.80e-17 | -2.33e-02 | -0.0272 |
64759 | TNS3 | A002-C-021 | Human | Colorectum | FAP | 2.33e-06 | 3.85e-01 | 0.1171 |
64759 | TNS3 | A002-C-205 | Human | Colorectum | FAP | 4.32e-23 | 3.25e-02 | -0.1236 |
64759 | TNS3 | A001-C-104 | Human | Colorectum | FAP | 8.02e-04 | 1.15e-01 | 0.0184 |
64759 | TNS3 | A015-C-005 | Human | Colorectum | FAP | 1.40e-03 | 2.58e-01 | -0.0336 |
64759 | TNS3 | A015-C-006 | Human | Colorectum | FAP | 3.87e-15 | -1.68e-01 | -0.0994 |
64759 | TNS3 | A015-C-106 | Human | Colorectum | FAP | 4.37e-13 | 7.37e-02 | -0.0511 |
Page: 1 2 3 4 5 6 7 |
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∗log2FC in expression of this searched gene in stem-like cells from each diseased tissue sample relative to stem-like cells in normal samples in each tissue plotted against the malignancy continuum. Samples are colored based on if they are from different disease stage. |
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Malignant transformation related pathway analysis |
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Tissue | Disease Stage | Enriched GO biological Processes |
Colorectum | AD | ![]() |
Colorectum | SER | ![]() |
Colorectum | MSS | ![]() |
Colorectum | MSI-H | ![]() |
Colorectum | FAP | ![]() |
∗Top 15 enriched GO BP terms are showed in the bar plot of each disease state in each tissue. Each row represents a significant GO biological process which is colored according to the -log10(p.adjust). |
Page: 1 2 3 4 5 6 7 8 9 |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:0016311 | Colorectum | AD | dephosphorylation | 123/3918 | 417/18723 | 1.84e-05 | 3.82e-04 | 123 |
GO:00163112 | Colorectum | MSS | dephosphorylation | 101/3467 | 417/18723 | 1.98e-03 | 1.70e-02 | 101 |
GO:00163113 | Colorectum | FAP | dephosphorylation | 95/2622 | 417/18723 | 7.07e-07 | 3.32e-05 | 95 |
GO:00163114 | Colorectum | CRC | dephosphorylation | 79/2078 | 417/18723 | 1.27e-06 | 7.21e-05 | 79 |
GO:001631110 | Esophagus | ESCC | dephosphorylation | 251/8552 | 417/18723 | 1.26e-09 | 2.99e-08 | 251 |
GO:00163115 | Liver | NAFLD | dephosphorylation | 69/1882 | 417/18723 | 2.27e-05 | 6.23e-04 | 69 |
GO:001631111 | Liver | Cirrhotic | dephosphorylation | 130/4634 | 417/18723 | 1.58e-03 | 1.03e-02 | 130 |
GO:001631121 | Liver | HCC | dephosphorylation | 230/7958 | 417/18723 | 1.00e-07 | 1.96e-06 | 230 |
GO:00163118 | Prostate | BPH | dephosphorylation | 98/3107 | 417/18723 | 1.53e-04 | 1.35e-03 | 98 |
GO:001631113 | Prostate | Tumor | dephosphorylation | 98/3246 | 417/18723 | 7.31e-04 | 5.08e-03 | 98 |
GO:001631116 | Thyroid | PTC | dephosphorylation | 174/5968 | 417/18723 | 1.20e-05 | 1.31e-04 | 174 |
GO:001631117 | Thyroid | ATC | dephosphorylation | 179/6293 | 417/18723 | 3.88e-05 | 3.15e-04 | 179 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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Cell-cell communication analysis |
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Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
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TF | Cell Type | Tissue | Disease Stage | Target Gene | RSS | Regulon Activity |
∗The dot plots of a searched regulon are shown for all cell subpopulations in each disease state of each tissue based on the regulon specific score inferred using pySCENIC and by calculating the average expression. |
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Somatic mutation of malignant transformation related genes |
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Hugo Symbol | Variant Class | Variant Classification | dbSNP RS | HGVSc | HGVSp | HGVSp Short | SWISSPROT | BIOTYPE | SIFT | PolyPhen | Tumor Sample Barcode | Tissue | Histology | Sex | Age | Stage | Therapy Types | Drugs | Outcome |
TNS3 | SNV | Missense_Mutation | novel | c.980T>C | p.Leu327Pro | p.L327P | Q68CZ2 | protein_coding | deleterious(0) | probably_damaging(0.936) | TCGA-B5-A3FC-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
TNS3 | SNV | Missense_Mutation | c.2225N>T | p.Ala742Val | p.A742V | Q68CZ2 | protein_coding | tolerated(0.5) | benign(0) | TCGA-BG-A0M4-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | SD | |
TNS3 | SNV | Missense_Mutation | novel | c.1732N>A | p.Ala578Thr | p.A578T | Q68CZ2 | protein_coding | tolerated(0.26) | benign(0.003) | TCGA-BK-A13B-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | PD |
TNS3 | SNV | Missense_Mutation | c.232G>A | p.Ala78Thr | p.A78T | Q68CZ2 | protein_coding | tolerated(0.24) | probably_damaging(0.996) | TCGA-BK-A6W3-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
TNS3 | SNV | Missense_Mutation | novel | c.5N>G | p.Glu2Gly | p.E2G | Q68CZ2 | protein_coding | deleterious(0) | benign(0.255) | TCGA-BS-A0UF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
TNS3 | SNV | Missense_Mutation | novel | c.652N>A | p.Val218Ile | p.V218I | Q68CZ2 | protein_coding | tolerated(0.67) | benign(0.009) | TCGA-D1-A16V-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
TNS3 | SNV | Missense_Mutation | novel | c.909N>T | p.Glu303Asp | p.E303D | Q68CZ2 | protein_coding | deleterious(0.01) | possibly_damaging(0.609) | TCGA-D1-A16X-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
TNS3 | SNV | Missense_Mutation | c.1133N>G | p.Asn378Ser | p.N378S | Q68CZ2 | protein_coding | tolerated(1) | benign(0) | TCGA-D1-A17F-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
TNS3 | SNV | Missense_Mutation | rs552081357 | c.1598C>T | p.Pro533Leu | p.P533L | Q68CZ2 | protein_coding | tolerated(0.37) | benign(0) | TCGA-D1-A2G0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
TNS3 | SNV | Missense_Mutation | novel | c.2984C>A | p.Ala995Asp | p.A995D | Q68CZ2 | protein_coding | tolerated(0.12) | benign(0.08) | TCGA-DF-A2KN-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | Unknown | I/II | Unknown | Unknown | SD |
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Related drugs of malignant transformation related genes |
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(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
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